HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylamine → Indole, 3-((dimethylamino)methyl)-7-nitro-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 7-Nitroindole | HCID 23396 | — |
| Solvent | Water | HCID 962 | — |
| Product | Indole, 3-((dimethylamino)methyl)-7-nitro- | HCID 15451 | — |
Reaction Steps
A mixture of 7-nitro-1H-indole (3 g, 18.5 mmol), 40% aqueous dimethylamine (3.12 mL, 27.7 mmol) and 37% aqueous formaldehyde (1.57 mL, 19.3 mmol) was stirred for three days at ambient temperature. The reaction mixture was diluted with H2O (20 mL) followed 15% aqueous NaOH (200 mL) and extracted with CHCl3 (3×200 mL). The combined organic extracts were dried over Na2SO4, filtered, and concentrated in vacuo to give the title compound in sufficient purity for use in the next step. MS: m/z=181 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08133891B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-eefad590ec4b4118a09d6d9a1d516ac2 |
| Source note | uspto-grants-2012_03 |